A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6526194



Internal ID20899555
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:3179456..3181648hg38UCSC Ensembl
chr20:3160102..3162294hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg382193
hg192193
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18067372
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6526194
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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